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Jens Vuust

Showing results (1-10 of 15) with videos related to

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Current Protocols in Human Genetics|April 23, 2008
Single-strand conformation polymorphism analysis using capillary electrophoresisLars Allan Larsen, Michael Christiansen, Jens Vuust, et al.
Aesthetic Plastic Surgery|March 11, 2005
Adverse reactions to injectable soft tissue permanent fillersLise Christensen, Vibeke Breiting, Martin Janssen, et al.
Human Mutation|April 4, 2003
Capillary electrophoresis-based single strand DNA conformation analysis in high-throughput mutation screeningPaal Skytt Andersen, Cathrine Jespersgaard, Jens Vuust, et al.
Human Mutation|January 29, 2003
High-throughput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: validation of the methodPaal Skytt Andersen, Cathrine Jespersgaard, Jens Vuust, et al.
Ugeskrift for Laeger|October 31, 2006
[Screening for fragile X syndrome. International experiences]Jens Vuust, Lars Allan Larsen, Karen Grønskov, et al.
FEMS Microbiology Letters|September 29, 2004
Identification and molecular characterization of the gene encoding coli surface antigen 20 of enterotoxigenic Escherichia coliHåvard Valvatne, Hans Steinsland, Harleen M S Grewal, et al.
Genetic Testing|March 31, 2007
Whole genome amplification on DNA from filter paper blood spot samples: an evaluation of selected systemsKarina Meden Sørensen, Cathrine Jespersgaard, Jens Vuust, et al.
Cardiovascular Research|February 5, 2003
Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutationsOle Havndrup, Henning Bundgaard, Paal Skytt Andersen, et al.
Gynecologic Oncology|September 27, 2005
P53 mutations in tissue from Danish ovarian cancer patients: from the Danish "MALOVA" ovarian cancer studyEstrid V S Høgdall, Susanne K Kjaer, Jan Blaakaer, et al.
European Journal of Human Genetics : EJHG|October 16, 2004
One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod regionLotte Hougs, Ole Havndrup, Henning Bundgaard, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Current Protocols in Human Genetics|April 23, 2008
Single-strand conformation polymorphism analysis using capillary electrophoresisLars Allan Larsen, Michael Christiansen, Jens Vuust, et al.
Aesthetic Plastic Surgery|March 11, 2005
Adverse reactions to injectable soft tissue permanent fillersLise Christensen, Vibeke Breiting, Martin Janssen, et al.
Human Mutation|April 4, 2003
Capillary electrophoresis-based single strand DNA conformation analysis in high-throughput mutation screeningPaal Skytt Andersen, Cathrine Jespersgaard, Jens Vuust, et al.
Human Mutation|January 29, 2003
High-throughput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: validation of the methodPaal Skytt Andersen, Cathrine Jespersgaard, Jens Vuust, et al.
Ugeskrift for Laeger|October 31, 2006
[Screening for fragile X syndrome. International experiences]Jens Vuust, Lars Allan Larsen, Karen Grønskov, et al.
FEMS Microbiology Letters|September 29, 2004
Identification and molecular characterization of the gene encoding coli surface antigen 20 of enterotoxigenic Escherichia coliHåvard Valvatne, Hans Steinsland, Harleen M S Grewal, et al.
Genetic Testing|March 31, 2007
Whole genome amplification on DNA from filter paper blood spot samples: an evaluation of selected systemsKarina Meden Sørensen, Cathrine Jespersgaard, Jens Vuust, et al.
Cardiovascular Research|February 5, 2003
Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutationsOle Havndrup, Henning Bundgaard, Paal Skytt Andersen, et al.
Gynecologic Oncology|September 27, 2005
P53 mutations in tissue from Danish ovarian cancer patients: from the Danish "MALOVA" ovarian cancer studyEstrid V S Høgdall, Susanne K Kjaer, Jan Blaakaer, et al.
European Journal of Human Genetics : EJHG|October 16, 2004
One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod regionLotte Hougs, Ole Havndrup, Henning Bundgaard, et al.
Pageof 2